HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1086268Generated: November 3, 2026
1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride → HCID 131716919, compound
https://huagongshe.com/reaction/1086268
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | 2-(1,2,3,4-Tetrahydronaphthalen-2-yl)acetic acid | HCID 10012739 | — |
| Reactant | Ethyl (4R)-4-thiazolidinecarboxylate | HCID 13011878 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 131716919 | HCID 131716919 | 68.5% |
Reaction Steps
To a mixture of 2.85 g of 1,2,3,4-tetrahydronaphthalen-2-ylacetic acid and 13.45 g of WSC.HCl was added 45 ml of methylene chloride under ice-cooling. The mixture was stirred for 5 minutes at room temperature. To this was added a solution of 2.4 g of L-thioproline ethyl ester in 7 ml of methylene chloride at room temperature, and the mixture was stirred for a further 18 hours at the same temperature. The reaction mixture was washed with water, diluted hydrochloric acid, and saturated sodium hydrogen carbonate in this order. The organic layer was dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue thus obtained was purified by silica gel column chromatography to produce 3.4 g of 3-(1,2,3,4-tetrahydronaphthalen-2-ylacetyl)-L-thioproline ethyl ester as a colorless oil (yield: 68%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05028604 |
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| Source dataset | uspto-grants-1991_07 |
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| ORD ID | ord-a66faf0c329b428184a153c0d46eec24 |
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| Source note | uspto-grants-1991_07 |
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